TUMOR OXYGENATION AFTER (1) CARBOGEN AND/OR PERFLUBRON EMULSION ADMINISTRATION IN TUMOR XENOGRAFTS (2) CARBOGEN ADMINISTRATION IN PATIENTS

被引:6
作者
GUICHARD, M
LARTIGAU, E
MARTIN, L
THOMAS, C
WEEGER, P
LAMBIN, P
LERIDANT, AM
LUSINCHI, A
WIBAULT, P
LUBOINSKI, B
ESCHWEGE, F
机构
[1] INST GUSTAVE ROUSSY,DEPT CHIRURG CERV FACIALE,F-94804 VILLEJUIF,FRANCE
[2] INST GUSTAVE ROUSSY,DEPT RADIOTHERAPIE,F-94804 VILLEJUIF,FRANCE
来源
ARTIFICIAL CELLS BLOOD SUBSTITUTES AND IMMOBILIZATION BIOTECHNOLOGY | 1994年 / 22卷 / 04期
关键词
D O I
10.3109/10731199409138837
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This study examines the changes in tumor pO(2) distribution assessed by polarography (KIMOC 6650, Eppendorf) in 1) two human tumor xenografts after carbogen inhalation with or without a perflubron (perfluorooctylbromide) emulsion (Oxygent(TM), Alliance Pharmaceutical corp.) and in 2) human head and neck carcinomas after carbogen inhalation. Mice bearing HRT18 or NA11+ tumors were restrained and their body temperature was kept constant. Perflubron emulsion (4 ml/kg) was injected i.v. in the mice. In patients, oxygenation of the head and neck metastatic lymph nodes was assessed before and/or during carbogen exposure. The distribution of pO(2) values shifted upwards during carbogen exposure in both animals and patients while the proportion of low pO(2) values decreased. The maximal effect was obtained with patients after 1 to 6 minutes of carbogen exposure, but 4 patients still maintained very low pO(2)s. Carbogen plus 4 ml/kg perflubron emulsion was more efficient than carbogen alone for increasing hypoxic tumor pO(2) in animals. If the animals data could be extrapolated to humans, then the effect of carbogen on tumor oxygenation should be increased by perflubron emulsion administration.
引用
收藏
页码:1355 / 1360
页数:6
相关论文
共 10 条
[2]  
LARTIGAU E, 1993, CANCER-AM CANCER SOC, V71, P2319, DOI 10.1002/1097-0142(19930401)71:7<2319::AID-CNCR2820710724>3.0.CO
[3]  
2-C
[4]   FLUOROCARBON-BASED INVIVO OXYGEN-TRANSPORT AND DELIVERY SYSTEMS [J].
RIESS, JG .
VOX SANGUINIS, 1991, 61 (04) :225-239
[5]   DEVELOPMENT OF HIGHLY FLUID, CONCENTRATED AND STABLE FLUOROCARBON EMULSIONS FOR DIAGNOSIS AND THERAPY [J].
RIESS, JG ;
DALFORS, JL ;
HANNA, GK ;
KLEIN, DH ;
KRAFFT, MP ;
PELURA, TJ ;
SCHUTT, EG .
BIOMATERIALS ARTIFICIAL CELLS AND IMMOBILIZATION BIOTECHNOLOGY, 1992, 20 (2-4) :839-842
[6]  
RIESS JG, 1993, BLOOD SUBSTITUTES OX, P24
[7]   MODULATION OF TUMOR OXYGENATION AND RADIOSENSITIVITY BY A PERFLUOROOCTYLBROMIDE EMULSION [J].
ROCKWELL, S ;
KELLEY, M ;
IRVIN, CG ;
HUGHES, CS ;
PORTER, E ;
YABUKI, H ;
FISCHER, JJ .
RADIOTHERAPY AND ONCOLOGY, 1991, 22 (02) :92-98
[8]   IMPORTANCE OF PRE-IRRADIATION BREATHING TIMES OF OXYGEN AND CARBOGEN (5-PERCENT CO2 - 95-PERCENT O-2) ON INVIVO RADIATION RESPONSE OF A MURINE SARCOMA [J].
SIEMANN, DW ;
HILL, RP ;
BUSH, RS .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1977, 2 (9-10) :903-911
[9]   NEW HIGH O2 CARRYING PERFLUOROCHEMICAL EMULSIONS AND OR CARBOGEN - REACTIONS OF A HUMAN-TUMOR XENOGRAFT TO IRRADIATION [J].
THOMAS, C ;
LARTIGAU, E ;
MALAISE, EP ;
GUICHARD, M .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1989, 16 (05) :1157-1160
[10]  
VAUPEL P, 1990, STRAHLENTHER ONKOL, V166, P377